The Safety Rates Drug Report

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Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
121999695 12199969 5 F 20160127 20160701 20160322 20160711 EXP GB-MYLANLABS-2016M1011289 MYLAN 0.00 Y 0.00000 20160711 OT GB GB

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
121999695 12199969 1 SS DOCETAXEL MYLAN DOCETAXEL 1 Unknown UNK U U 0
121999695 12199969 2 PS EPIRUBICIN EPIRUBICIN 1 Unknown UNK (UNK) U U 91599
121999695 12199969 3 SS ZOLEDRONIC ACID ZOLEDRONIC ACID 1 Unknown UNK U U 0
121999695 12199969 4 SS ONDANSETRON ONDANSETRON 1 Unknown UNK U U 0
121999695 12199969 5 SS Calcium Carbonate MYLAN CALCIUM CARBONATE 1 Unknown U U 0
121999695 12199969 6 SS NEULASTA PEGFILGRASTIM 1 Unknown UNK (UNK, CYCLE 2 DAY 9) U U 0
121999695 12199969 7 SS APREPITANT DCI APREPITANT 1 Unknown UNK U U 0
121999695 12199969 8 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown UNK U U 0
121999695 12199969 9 SS LEVOMEPROMAZINE /00038602/ LEVOMEPROMAZINE 1 Unknown UNK U U 0
121999695 12199969 10 SS METOCLOPRAMIDE /00041902/ METOCLOPRAMIDE HYDROCHLORIDE 1 Unknown UNK U U 0
121999695 12199969 11 SS TAXOTERE DOCETAXEL 1 UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121999695 12199969 2 Product used for unknown indication
121999695 12199969 3 Product used for unknown indication
121999695 12199969 4 Product used for unknown indication
121999695 12199969 6 Product used for unknown indication
121999695 12199969 7 Product used for unknown indication
121999695 12199969 8 Product used for unknown indication
121999695 12199969 9 Product used for unknown indication
121999695 12199969 10 Product used for unknown indication
121999695 12199969 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121999695 12199969 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121999695 12199969 Alopecia
121999695 12199969 Back pain
121999695 12199969 Constipation
121999695 12199969 Dysgeusia
121999695 12199969 Fatigue
121999695 12199969 Neuropathy peripheral
121999695 12199969 Paraesthesia oral
121999695 12199969 Phlebitis
121999695 12199969 Skin discolouration
121999695 12199969 Sunburn

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found